Informationen:
Fehler:
ID
39499
Beschreibung
Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through Monitoring in HF Patients (CONFIRM-HF); ODM derived from: https://clinicaltrials.gov/show/NCT02026635
Link
https://clinicaltrials.gov/show/NCT02026635
Stichworte
Versionen (1)
- 19.01.20 19.01.20 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
19. Januar 2020
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Heart Failure NCT02026635
Eligibility Heart Failure NCT02026635
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Heart Failure NCT02026635
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Age
Item
at least 18 years of age
boolean
C0001779 (UMLS CUI [1])
Admission Heart failure Worsening
Item
admission for worsening of hf
boolean
C0184666 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C0332271 (UMLS CUI [1,3])
C0018801 (UMLS CUI [1,2])
C0332271 (UMLS CUI [1,3])
Discharge to home
Item
discharged to home
boolean
C0184713 (UMLS CUI [1])
Cardiac implant device Specified
Item
have appropriate cardiac device with optivol® implanted for at least 34 days prior to enrollment
boolean
C0581396 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,2])
Enrollment Cardiac implant device System Specified | Ability Data Transmission
Item
enrolled in carelink® system and able to transmit data
boolean
C1516879 (UMLS CUI [1,1])
C0581396 (UMLS CUI [1,2])
C0449913 (UMLS CUI [1,3])
C0205369 (UMLS CUI [1,4])
C0085732 (UMLS CUI [2,1])
C0332289 (UMLS CUI [2,2])
C0581396 (UMLS CUI [1,2])
C0449913 (UMLS CUI [1,3])
C0205369 (UMLS CUI [1,4])
C0085732 (UMLS CUI [2,1])
C0332289 (UMLS CUI [2,2])
Ability Participation Duration
Item
able to participate for at least 3 months
boolean
C0085732 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C0679823 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Status post Heart Transplantation | Patient on waiting list
Item
post heart transplant or actively listed
boolean
C0231290 (UMLS CUI [1,1])
C0018823 (UMLS CUI [1,2])
C0422768 (UMLS CUI [2])
C0018823 (UMLS CUI [1,2])
C0422768 (UMLS CUI [2])
Heart failure End-stage | Inotropic agent chronic | Left ventricular assist device Support
Item
end-stage (stage d) hf, including treatment with chronic ionotropic drugs or left ventricular assist device support
boolean
C0018801 (UMLS CUI [1,1])
C0205088 (UMLS CUI [1,2])
C0304509 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C0181598 (UMLS CUI [3,1])
C1521721 (UMLS CUI [3,2])
C0205088 (UMLS CUI [1,2])
C0304509 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C0181598 (UMLS CUI [3,1])
C1521721 (UMLS CUI [3,2])
Renal dysfunction chronic Stage | Glomerular Filtration Rate
Item
stage iv or v chronic renal dysfunction (gfr <25 mol/min per 1.73 m2)
boolean
C3279454 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C1306673 (UMLS CUI [1,3])
C0017654 (UMLS CUI [2])
C0205191 (UMLS CUI [1,2])
C1306673 (UMLS CUI [1,3])
C0017654 (UMLS CUI [2])
Severe chronic obstructive pulmonary disease | Requirement Home oxygen therapy
Item
severe chronic obstructive pulmonary disease (copd) requiring home oxygen
boolean
C0730607 (UMLS CUI [1])
C1514873 (UMLS CUI [2,1])
C1960973 (UMLS CUI [2,2])
C1514873 (UMLS CUI [2,1])
C1960973 (UMLS CUI [2,2])
Pulmonary hypertension, severe | Independent of Left-Sided Heart Failure
Item
severe pulmonary hypertension not due to left-sided hf
boolean
C2750273 (UMLS CUI [1])
C0332291 (UMLS CUI [2,1])
C0023212 (UMLS CUI [2,2])
C0332291 (UMLS CUI [2,1])
C0023212 (UMLS CUI [2,2])